Recalls distributed in Alabama
These notices name Alabama in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.
3,229 stored notices name Alabama, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Alabama too — those are in the archive.
Reported Apr 11, 2018
HydroSil Gripper Intermittent Catheters- 10" lengths - 30 catheters per box, each catheter is packaged in an individual…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 11, 2018
King Arthur Flour, 100% Organic, Finely Ground, Coconut Flour, UPC 0 71012 10702 5, Distributed by: The King Arthur…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The King Arthur Flour Company, Inc.
FDA (openFDA food enforcement)
Reported Apr 4, 2018
Rechargeable Li-ion battery used with Puritan Bennett TM 980 Series Ventilator System including Pediatric-Adult…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 4, 2018
(1) Sigma HP Cemented Trochlea Size 1 Narrow Left, Catalog Number: 102403100, GTIN: 10603295001614; (2) Sigma HP…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Apr 4, 2018
Sonimage HS1 Ultrasound Kit AC adapter, Product Number: A7AP, UDI: 04560141940031
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Konica Minolta Medical Imaging USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 4, 2018
8F Plastic Dignity¿ Low Profile CT Port W/Pre-Attached ChronoFlex¿ Polyurethane Catheter
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Components, Inc. dba MedComp
FDA (openFDA device enforcement)
Reported Apr 4, 2018
Gas Module 3 monitoring spirometer, Part Number: 115-030108-00 Product Usage: The Gas Module 3 is an accessory device…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Mindray DS USA, Inc. dba Mindray North America
FDA (openFDA device enforcement)
Reported Apr 4, 2018
Maurice's Honey Southern Gold BBQ Sauce; Net Wt. 18 oz. bottles; UPC Code 0 7561654332 6 and Carolina Gold Honey Sauce;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Piggie Park Enterprises Inc.
FDA (openFDA food enforcement)
Reported Apr 4, 2018
The FEMTO LDV(TM)Z8 Femtosecond Surgical Laser The FEMTO LDV(TM)Z8 Femtosecond Surgical Laser is an ophthalmic surgical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SIE AG, Surgical Instrument Engineering
FDA (openFDA device enforcement)
Reported Apr 4, 2018
Southgate Hot Dog Chili Sauce 15 oz cans UPC 0 71846 95242
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vietti Acquisitions, LLC
FDA (openFDA food enforcement)
Reported Mar 31, 2018
PFP Enterprises LLC Retira Productos De Carne De Res Cruda Producidos Sin El Beneficio De La Inspeccin
High riskUsing this product could cause serious injury, illness or death — stop using it now.Patterson TMP Operating, LLC
USDA FSIS
Reported Mar 28, 2018
BD Vacutainer¿ EDTA Lavender Top Tubes: Catalog Numbers: 1. 366401 (UDI: 50382903664011); 2. 366450 (UDI:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Becton Dickinson & Company
3 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 28, 2018
Malecot Nephrostomy Catheter System, Product Number: M001224110, GTIN: 08714729030980 The Malecot and the Stenting…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
6 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 28, 2018
CATHETER REPAIR KIT, REF AAC52001, UDI 884908001891 Product Usage: The Medcomp Repair Kit is indicated for use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Components, Inc. dba MedComp
9 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 28, 2018
Artis one fluoroscopic x-ray system and patient table Artis one is an angiography system developed for diagnostic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 21, 2018
Difco" Agar Noble, 500g bottle Noble Agar is a solidifying agent that is essentially free of impurities. It is used in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Mar 21, 2018
Kodiak Cakes, Energy Waffles, Blueberry Chia, Net Wt 10.72 Oz (304 g), Kodiak Cakes, Park City, UT. Packaging…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kodiak Cakes, LLC
FDA (openFDA food enforcement)
Reported Mar 21, 2018
OneStep CPR Complete, Adult Multi Function Electrodes, Part Numbers: 8900 0214 01 (case of 8 single electrodes, UDI:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ZOLL Medical Corporation
FDA (openFDA device enforcement)
Reported Mar 14, 2018
i-STAT DE handheld data processing module for clinical use, Software Version 2.8, List Number:08K46-01115200 (UDI:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Point Of Care Inc.
FDA (openFDA device enforcement)
Reported Mar 14, 2018
O-arm¿ O2 interventional fluoroscopic x-ray system; Catalog Number: B1-700-02000 The O-arm O2 Imaging System is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.-Littleton
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 14, 2018
Medtronic Synchromed II Model 8637 supplied in 20mL and 40 mL reservoir size and a catheter. Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Mar 14, 2018
cobas 6000 Modular Series system; Part Numbers: 1. 04745914001 cobas c 501 module; 2. 05036453001 cobas 6000 UL c 501 +…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 14, 2018
2.5 mm Reaming Rod, Ball tip, 950 mm, sterile, Part Number: 351.706S Reaming Rods are intended for guiding of reamers…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
6 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 14, 2018
Flexible Shaft hip and anatomical shoulder instrument used for preparation of bone in Trauma, Hip and Shoulder…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new Alabama recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
Other states
RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.